Canonical Allele Identifier: PA2826464692
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421094
ClinVar RCV Id: RCV000484616 RCV001013177 RCV001205685
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn530His
CA16617589
NM_001258281.1:c.1588A>C